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Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar

Countries in the Greater Mekong Subregion have committed to eliminate Plasmodium falciparum malaria by 2025. Subclinical malaria infections that can be detected by highly sensitive polymerase chain reaction (PCR) testing in asymptomatic individuals represent a potential impediment to this goal, alth...

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Autores principales: Egger, Joseph R., Han, Kay T., Fang, Huang, Zhou, Xiao Nong, Hlaing, Tin M., Thant, Myo, Han, Zay Y., Wang, Xiao X., Hong, Tu, Platt, Alyssa, Simmons, Ryan, Thane, Thynn K., Meng, Manfred, Hogue, Joyce, Markwalter, Christine F., Thi, Aung, Htay, Thura, Thein, Zaw W., Paing, Aye K., Tun, Zin M., Oo, Swai M., Aung, Poe P., Nyunt, Myaing M., Plowe, Christopher V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society of Tropical Medicine and Hygiene 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490656/
https://www.ncbi.nlm.nih.gov/pubmed/35895341
http://dx.doi.org/10.4269/ajtmh.22-0027
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author Egger, Joseph R.
Han, Kay T.
Fang, Huang
Zhou, Xiao Nong
Hlaing, Tin M.
Thant, Myo
Han, Zay Y.
Wang, Xiao X.
Hong, Tu
Platt, Alyssa
Simmons, Ryan
Thane, Thynn K.
Meng, Manfred
Hogue, Joyce
Markwalter, Christine F.
Thi, Aung
Htay, Thura
Thein, Zaw W.
Paing, Aye K.
Tun, Zin M.
Oo, Swai M.
Aung, Poe P.
Nyunt, Myaing M.
Plowe, Christopher V.
author_facet Egger, Joseph R.
Han, Kay T.
Fang, Huang
Zhou, Xiao Nong
Hlaing, Tin M.
Thant, Myo
Han, Zay Y.
Wang, Xiao X.
Hong, Tu
Platt, Alyssa
Simmons, Ryan
Thane, Thynn K.
Meng, Manfred
Hogue, Joyce
Markwalter, Christine F.
Thi, Aung
Htay, Thura
Thein, Zaw W.
Paing, Aye K.
Tun, Zin M.
Oo, Swai M.
Aung, Poe P.
Nyunt, Myaing M.
Plowe, Christopher V.
author_sort Egger, Joseph R.
collection PubMed
description Countries in the Greater Mekong Subregion have committed to eliminate Plasmodium falciparum malaria by 2025. Subclinical malaria infections that can be detected by highly sensitive polymerase chain reaction (PCR) testing in asymptomatic individuals represent a potential impediment to this goal, although the extent to which these low-density infections contribute to transmission is unclear. To understand the temporal dynamics of subclinical malaria in this setting, a cohort of 2,705 participants from three epidemiologically distinct regions of Myanmar was screened for subclinical P. falciparum and P. vivax infection using ultrasensitive PCR (usPCR). Standard rapid diagnostic tests (RDTs) for P. falciparum were also performed. Individuals who tested positive for malaria by usPCR were followed for up to 12 weeks. Regression analysis was performed to estimate whether the baseline prevalence of infection and the count of repeated positive tests were associated with demographic, behavioral, and clinical factors. At enrollment, the prevalence of subclinical malaria infection measured by usPCR was 7.7% (1.5% P. falciparum monoinfection, 0.3% mixed P. falciparum and P. vivax, and 6.0% P. vivax monoinfection), while P. falciparum prevalence measured by RDT was just 0.2%. Prevalence varied by geography and was higher among older people and in those with outdoor exposure and travel. No difference was observed in either the prevalence or count of subclinical infection by time of year, indicating that even in low-endemicity areas, a reservoir of subclinical infection persists year-round. If low-density infections are shown to represent a significant source of transmission, identification of high-risk groups and locations may aid elimination efforts.
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spelling pubmed-94906562022-09-28 Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar Egger, Joseph R. Han, Kay T. Fang, Huang Zhou, Xiao Nong Hlaing, Tin M. Thant, Myo Han, Zay Y. Wang, Xiao X. Hong, Tu Platt, Alyssa Simmons, Ryan Thane, Thynn K. Meng, Manfred Hogue, Joyce Markwalter, Christine F. Thi, Aung Htay, Thura Thein, Zaw W. Paing, Aye K. Tun, Zin M. Oo, Swai M. Aung, Poe P. Nyunt, Myaing M. Plowe, Christopher V. Am J Trop Med Hyg Research Article Countries in the Greater Mekong Subregion have committed to eliminate Plasmodium falciparum malaria by 2025. Subclinical malaria infections that can be detected by highly sensitive polymerase chain reaction (PCR) testing in asymptomatic individuals represent a potential impediment to this goal, although the extent to which these low-density infections contribute to transmission is unclear. To understand the temporal dynamics of subclinical malaria in this setting, a cohort of 2,705 participants from three epidemiologically distinct regions of Myanmar was screened for subclinical P. falciparum and P. vivax infection using ultrasensitive PCR (usPCR). Standard rapid diagnostic tests (RDTs) for P. falciparum were also performed. Individuals who tested positive for malaria by usPCR were followed for up to 12 weeks. Regression analysis was performed to estimate whether the baseline prevalence of infection and the count of repeated positive tests were associated with demographic, behavioral, and clinical factors. At enrollment, the prevalence of subclinical malaria infection measured by usPCR was 7.7% (1.5% P. falciparum monoinfection, 0.3% mixed P. falciparum and P. vivax, and 6.0% P. vivax monoinfection), while P. falciparum prevalence measured by RDT was just 0.2%. Prevalence varied by geography and was higher among older people and in those with outdoor exposure and travel. No difference was observed in either the prevalence or count of subclinical infection by time of year, indicating that even in low-endemicity areas, a reservoir of subclinical infection persists year-round. If low-density infections are shown to represent a significant source of transmission, identification of high-risk groups and locations may aid elimination efforts. The American Society of Tropical Medicine and Hygiene 2022-09 2022-07-25 /pmc/articles/PMC9490656/ /pubmed/35895341 http://dx.doi.org/10.4269/ajtmh.22-0027 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Egger, Joseph R.
Han, Kay T.
Fang, Huang
Zhou, Xiao Nong
Hlaing, Tin M.
Thant, Myo
Han, Zay Y.
Wang, Xiao X.
Hong, Tu
Platt, Alyssa
Simmons, Ryan
Thane, Thynn K.
Meng, Manfred
Hogue, Joyce
Markwalter, Christine F.
Thi, Aung
Htay, Thura
Thein, Zaw W.
Paing, Aye K.
Tun, Zin M.
Oo, Swai M.
Aung, Poe P.
Nyunt, Myaing M.
Plowe, Christopher V.
Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar
title Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar
title_full Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar
title_fullStr Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar
title_full_unstemmed Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar
title_short Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar
title_sort temporal dynamics of subclinical malaria in different transmission zones of myanmar
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490656/
https://www.ncbi.nlm.nih.gov/pubmed/35895341
http://dx.doi.org/10.4269/ajtmh.22-0027
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